Structure, thermal-stability and reducibility of Si-doped Ce–Zr–O solid solution

The Si-doped Ce–Zr–O solid solutions have been prepared by the reverse microemulsion method. The effects of Si and its content on the structure characters, thermal-stability and reducibility of the Ce–Zr–O solid solution have been studied by N₂ adsorption, XRD, laser Raman (LR), TPR, FT-IR, NMR and XPS methods. The results indicate that, there are the bonds of Si–O–M (Ce or Zr) in the Ce–Zr–Si–O solid solutions, and the presence of Si can increase obviously the surface area, thermal-stability, crystal lattice distortion rate, and reducibility of the solid solution. The surface area of the sample with 20 wt.% Si reaches 153 m² g⁻¹ after being calcined at 900 °C for 6 h. The Ce–Zr–O solid solution with 5.2–10 wt.% Si shows excellent thermal-stability and reducibility.     

氯酸钠-硫磺法制二氧化氯的研究

对硫磺还原氯酸钠制备二氧化氯的工艺条件进行了研究 ,反应的最佳条件是 :温度为 60～70℃ ,氯酸钠浓度为 4～ 5 mol/L,反应液中维持硫酸浓度为 1 mol/L以上。该法具有反应温和易于控制、硫酸消耗少、成本低廉和产品纯度高的优点     

基于容器的Web运行环境轻量级虚拟化方法

Web运行环境、Web服务及Web应用的虚拟化是减轻Web操作系统安全风险的一种有效方法,然而Web运行环境的虚拟化仍然存在不少挑战,如：执行时间、资源负载和兼容性等。为解决Web操作系统在安全性、执行时间、资源负载和兼容性方面的问题,提出了一种Web运行环境轻量级虚拟化方法,采用Docker容器技术实现进程级别的隔离。本虚拟化方法可在一个基本内核上支持运行多种Web运行环境的容器。此外,为了减轻容器创建负载,提出了容器启动机制;为减轻系统资源负载,进行了系统的轻量化处理。在嵌入式设备的实验结果表明,该虚拟化方法在执行时间、资源负载及兼容性方面都具有较优表现。     

从假性紫罗兰酮合成β-紫罗兰酮中主要副产物(I)的分离鉴定

假性紫罗兰酮在浓硫酸及 - 2 0°C低温条件下反应 ,主要生成 β-紫罗兰酮 ,少量的 α-及 γ-紫罗兰酮 ,同时生成副产物 ( I)及 ( II)。用 IR、1H NMR及 MS光谱分析方法 ,对副产物 ( I)进行了结构鉴定 ,结构为 3,4,4a,5 ,8,8a-六氢 - 2 ,5 ,5 ,8a-四甲基 - 2 H - 1 -苯并吡喃     

聚醚多元醇中间品钾（钠）离子的快速测定方法

本法采用乙醇水溶解试样，以经过处理的无钾，钠离子聚醚鸩元醇作为基体，配制标准样品，用火焰光度法检测聚醚多元醇中间品的钾（钠）离子的含量。由于样品处理简单，应用浓度直读取数据，可快速准确地测定试样，适用于聚醚多元醇生产过程中间品的检验。     

电解氧化法制取葡萄糖酸钠

研究了在无隔膜槽中电解氧化葡萄糖制取葡萄糖酸钠的方法，得出了最佳工艺条件，为电解法制取葡萄糖酸钠的工业化提供了依据。     

固体硫在超临界/近临界酸性流体中的溶解度(Ⅰ)实验研究

建立了1套静态法测定难挥发物质(固体或液体)在超临界/近临界流体中溶解度的实验装置,并测定了固体硫在近临界硫化氢、超临界CO_2、CH_4及富硫化氢酸性气体混合物中的溶解度数据,取得了较好的结果.     

NR/共沉型聚丁二烯橡胶并用胶性能研究

研究NR／共沉型聚丁二烯橡胶并用胶的性能。试验结果表明，随共沉型聚丁二烯橡胶用量的增大，NR／共沉型聚丁二烯橡胶并用胶门尼粘度增大，焦烧时间和正硫化时间延长；与NR、NR／BR9000并用胶及NR／BR9073并用胶相比，NR／共沉型聚丁二烯橡胶并用胶的生热低、抗湿滑性优良，耐磨性稍差，其它性能相差不大。     

A new core–shell type fluorinated acrylic and siliconated polyurethane hybrid emulsion

A novel core–shell type fluorinated acrylic and siliconated polyurethane (FSiPUA) hybrid emulsion was prepared by seeded emulsion polymerization using siliconated polyurethane (SiPU) as a seed and forming the structure with SiPU as a shell and the copolymer of butyl acrylate (BA) with 2,2,2-trifluoroethylmethacrylate (TFEMA) as a core. SiPU was synthesized using isophorone diisocyanate (IPDI), polytetramethylene ether glycol (PTMG), polypropylene glycol (PPG), dihydroxybutyl-terminated polydimethylsiloxane (PDMS), dimethylol propionic acid (DMPA), 1,6-hexanediol (HDO) and triethylamine (TEA). The contents of siloxane and fluorine were determined according to the feed ratio. Fourier transform infrared spectroscopy (FTIR) was used to identify the chain structure of SiPU and FSiPUA. Investigation of transmission electron microscopy (TEM) confirmed the core–shell structure of FSiPUA emulsion and gave the particle size at about 50 nm. The measurement results of water contact angles and the solvent absorptions in water and n-octane for cured films showed that the water and the oil repellency for FSiPUA had been improved significantly with a suitable content of fluorine and siloxane.     

The deposition of coke from methane on a Ni/MgAl2O4 catalyst

Temperature-programmed reaction techniques and Raman spectroscopy were used to characterize coke species deposited on a 5% Ni/MgAl₂O₄ catalyst for dry reforming of methane. The CH₄ temperature-programmed decomposition profiles showed that the ignited decomposition temperatures of CH₄ increased from 273 to 378 °C when MgAl₂O₄ replaced the catalyst support γ-Al₂O₃. The temperature-programmed oxidation, temperature-programmed hydrogenation and temperature-programmed CO₂ reaction profiles showed that there were three carbon species (i.e. C_α, C_β and C_γ) on the catalyst surface. Raman spectroscopy showed that C_γ was graphite-like carbon species, which was responsible for catalyst deactivation. The C_γ species was the most inactive species toward H₂ and O₂, while it was unexpectedly more active toward CO₂. The unique reactivity of CO₂ with different coke specie could be ascribed to the carbonate, bidentate and formate species formation on MgAl₂O₄ surface. These surface species enhanced the oxidation of C_γ species and thus contributed to the high stability of Ni/MgAl₂O₄ catalyst.